Post Graduate Institute of Medical Sciences Rohtak, Haryana 124001, India.
J Pediatr Surg. 2010 Jan;45(1):E13-6. doi: 10.1016/j.jpedsurg.2009.10.057.
In view of the rarity of the lesion, we describe 3 cases of aphallia associated with genitourinary and nongenitourinary anomalies. One case was associated with an anorectal malformation, whereas 2 had a normal anal opening. One patient with a normal anal opening had an associated rectal-urethro-fistula. Development of the phallus, clinical presentation of aphallia, associated anomalies, and an outline of the management is discussed along with a review of the literature.
鉴于该病变罕见，我们描述了 3 例与泌尿生殖和非泌尿生殖异常相关的无阴茎畸形。1 例合并直肠肛门畸形，2 例肛门开口正常。1 例肛门开口正常的患者伴有直肠尿道瘘。本文讨论了阴茎的发育、无阴茎畸形的临床表现、相关畸形以及处理概要，并对文献进行了回顾。
